Following up of production plan and assurance of quality according to cGMP, GDP, SOPs and BPR.
Check the availability of
production requirements (BPR, Materials, Headcount and Machines) to achieve the
Review of all documents
during all processes to assure applying of Good Documentation Practices.
Review, update and follow
up (SOP’s, BPR, Job Description, etc.) to meet GDP requirements.
Train the shift leader on
all function documents to achieve cGMP and GDP requirements.
Evaluate all employees on
understanding all documents to enhance their performance.
Attend and share in any
trials done in the function on new (Products, Materials, Ideas),
Troubleshooting and Validation to enhance processes.
B.Sc. Degree in Pharmaceutical Science.
Years of Experience:
8 February 2022
Application End Date:
22 February 2022